Using the modified CRISPR-Cas9 gene-editing system and a therapeutic strategy known as long-acting slow-effective release antiviral therapy (LASER ART), a team of researchers has eliminated replication-competent HIV-1 DNA from the genomes of living mice. Published in the journal Nature Communications, the study marks a critical step toward the development of a possible cure for human HIV infection. Scanning electron micrograph of HIV particles infecting...
